Canonical Allele Identifier: PA916034366
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 231188
ClinVar RCV Id: RCV000215037 RCV001042097 RCV003153502
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gly2496Glu
CA6266113
NM_001351834.2:c.7487G>A